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BIOPRO GLENOID COMPONENT W/ KEEL & W/ POSTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001046
510(k) Type
Traditional
Applicant
Biopro, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2000
Days to Decision
69 days
Submission Type
Statement

BIOPRO GLENOID COMPONENT W/ KEEL & W/ POSTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001046
510(k) Type
Traditional
Applicant
Biopro, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2000
Days to Decision
69 days
Submission Type
Statement